K-number	K003322
Device name	CODMAN BACTISEAL CATHETERS
Applicant	Codman & Shurtleff, Inc.
Product code	HCA
Device class	Class II
Decision date	Oct 1, 2001
Decision	Substantially Equivalent
Regulation	882.4100

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View the full FDA submission: accessdata.fda.gov

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CODMAN BACTISEAL CATHETERS

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